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Artigo em Inglês | MEDLINE | ID: mdl-31136852

RESUMO

Copper is a metal that participates in several essential reactions in living organisms, and it has been used as an inflammatory inducing agent in zebrafish larvae. In this study, we evaluated the effect P2X7 receptor and/or pannexin channel 1 (PANX-1) blockage in this inflammation model. To perform the experiments, 7 dpf larvae were exposed to 10 µM of copper and treated with 100 µM probenecid, PANX-1 inhibitor, and/or 300 nM A740003, a P2X7R selective antagonist. Larvae survival was assessed up to 24 h after treatments. The evaluation of larvae behavior was evaluated after acute (4 h) and chronic (24 h) exposure. The parameters of locomotor activity measured were: mobile time, average speed, distance and turn angle. We analyzed the gene expression of the P2X7 receptor, PANX1a and PANX1b channels and interleukins IL-10 and IL-1b after 24 h of treatment. Treatments did not decrease larval survival in the time interval studied. Changes in larvae locomotion were observed after the longest time of exposure to copper and the treatment with probenecid was able to reverse part of the effects caused by copper. No significant difference was observed in the oxidative stress assays and probenecid and copper treatment decrease partially PANX1a gene expression groups. The data presented herein shows the relevance of the blockage of P2X7-PANX-1 in copper-induced inflammation.


Assuntos
Conexinas/genética , Cobre/toxicidade , Inflamação/induzido quimicamente , Receptores Purinérgicos P2X7/genética , Proteínas de Peixe-Zebra/genética , Peixe-Zebra/metabolismo , Acetamidas/farmacologia , Animais , Conexinas/antagonistas & inibidores , Modelos Animais de Doenças , Feminino , Regulação da Expressão Gênica/efeitos dos fármacos , Inflamação/mortalidade , Interleucina-10/genética , Interleucina-1beta/genética , Larva/efeitos dos fármacos , Locomoção/efeitos dos fármacos , Masculino , Estresse Oxidativo , Probenecid/farmacologia , Antagonistas do Receptor Purinérgico P2X/toxicidade , Quinolinas/farmacologia , Peixe-Zebra/genética , Proteínas de Peixe-Zebra/antagonistas & inibidores
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